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About the role
Key responsibilities & impact- Lead the strategy, execution, and success of a complex, multi‑study clinical research portfolio
- Provide end‑to‑end portfolio leadership across the clinical trial lifecycle
- Set the direction for a diverse clinical portfolio
- Serve as a trusted senior partner to sponsors—leading governance, communications, and issue resolution
- Establish and sustain a strong operational rhythm that delivers visibility, accountability, and results
- Coach and develop high‑performing teams
Requirements
What you’ll need- Bachelor’s Degree required, Master’s Degree preferred
- 7+ years’ experience in clinical research or project management including prior people leadership including line management
- Minimum 2 years’ experience in an Associate Director or equivalent role managing multiple complex clinical studies concurrently
- Demonstrated experience managing clinical trials independently
- 10+ years’ clinical research experience, Medical Affairs, including cross-functional engagement and evidence-generation support (preferred)
- Pharma/CRO management experience (preferred)
- Experience supporting Investigator-Initiated Trials (IITs) including feasibility, start-up coordination, oversight and stakeholder alignment (preferred)
Benefits
Comp & perks- Comprehensive benefits to support physical, mental, and financial well-being
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchproject managementclinical trial managementevidence generationinvestigator-initiated trialsfeasibility assessmentstart-up coordinationstakeholder alignmentcross-functional engagementpeople leadership
Soft Skills
leadershipcommunicationcoachingteam developmentstrategic planningproblem-solvingoperational managementaccountabilityvisibilitygovernance
Certifications
Bachelor's DegreeMaster's Degree
